Canonical Allele Identifier: CA1548129252
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859872_56859874delinsCAG , CM000667.2:g.56859872_56859874delinsCAG GRCh38
NC_000005.9:g.56155699_56155701delinsCAG , CM000667.1:g.56155699_56155701delinsCAG GRCh37
NC_000005.8:g.56191456_56191458delinsCAG NCBI36
NG_031884.1:g.49800_49802delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.791_793delinsCAG MANE Select ENSP00000382423.3:p.Ser264=
ENST00000399503.3:c.791_793delinsCAG ENSP00000382423.3:p.Ser264=
NM_005921.1:c.791_793delinsCAG NP_005912.1:p.Ser264=
XM_005248519.3:c.413_415delinsCAG XP_005248576.2:p.Ser138=
XM_011543406.1:c.536_538delinsCAG XP_011541708.1:p.Ser179=
XM_011543407.1:c.791_793delinsCAG XP_011541709.1:p.Ser264=
XM_011543408.1:c.791_793delinsCAG XP_011541710.1:p.Ser264=
XM_017009484.1:c.380_382delinsCAG XP_016864973.1:p.Ser127=
XM_017009485.1:c.302_304delinsCAG XP_016864974.1:p.Ser101=
XR_001742068.2:n.822_824delinsCAG
NM_005921.2:c.791_793delinsCAG MANE Select NP_005912.1:p.Ser264=